AccessGUDID - DEVICE: Green Guard Five-Shelf First Ad Cabinet (00347682011802)

GUDID

Device Identifier (DI) Information

Brand Name: Green Guard Five-Shelf First Ad Cabinet
Version or Model: 1180
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 1180
Company Name: Greenguard

Primary DI Number: 00347682011802
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 176528040 *Terms of Use

Device Description: 1181 -1.000 EACH 5 Shelf Cabinet Empty w/Pocket 3101 -1.000 EACH GG Tri-Antibiotic Ointment(25) 6400 -2.000 EACH GG Triangular Bandage + 2224 -1.000 EACH Maximum Non Aspirin (100) 3302- 2.000 EACH GG Cold Pack Medium/Boxed + 3103 -1.000 EACH GG Hydrocortisone Cream (25) 6102 -1.000 EACH 2" RIP-N-WRAP 6202 -1.000 EACH GG 2x2 Gauze Pads (25) 6304 -1.000 EACH GG Knuckle Bndg (40) + 6306 -1.000 EACH GG 2x3 Large Patch Bndg (25) 6302 -1.000 EACH GG Fingertip Bndg (40) + 6300 -2.000 EACH GG 7/8x3 Fabric Strip Bndg(50) 6310 -1.000 EACH GG Small Strip Bndg (50) + 3300- 1.000 EACH GG Cold Pack Large/Boxed + 6112 -2.000 EACH 2" Stretch Roller Gauze NS 6113 -2.000 EACH 3" Stretch Roller Gauze 3015 -1.000 EACH GG Alcohol Swabs (50) 6206 -1.000 EACH GG 3x3 Gauze Pads (25) 6213 -4.000 EACH 5x9 Combine Dressing ABD 3005 -1.000 GG Cold Spray 4 oz 4106 -1.000 EACH GG 8oz Eye Wash 2210 - 1.000 EACH Pain & Ache relief (250) 6603 -1.000 EACH Cotton Tip Appl 3" 100/Vial+ 6314 -1.000 EACH GG 1x3 Plastic Strip Bndg (60) 6248 -1.000 EACH Tape Tri-Cut Waterproof + 4150 -1.000 EACH Eye Cups in Vial 6/VL 17818 -1.000 EACH Cherry Benzocaine (18) Blis 2216 -STD 1.000 EACH Cough & Cold relief (100) 2280 - 1.000 EACH GG Max Str Somach relief 100ct 6520- 1.000 EACH-Emergency Large Wound Dressing 3004 -01.000 EACH GG Hydrogen Peroxide 2oz pump 8070 - 1.000 EACH Emergency CPR Kit 1220 -1.000 EACH Bodily Fluid Clean Up Kit 1180PI - 1.000 EACH Pocket Items 5 Shelf Kit 3001 -1.000 EACH GG Antiseptic Spray 2oz pump 6252 -1.000 EACH Tape 1/2" X 2 1/2 Y

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	Yes
Kit:	Yes
Combination Product:	Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
44039	First aid kit, medicated	A convenient collection of equipment, materials and pharmaceuticals intended to be used in an emergency for the rapid, initial treatment of an injury. It is typically used by emergency medical services (EMS), hospitals, institutions, schools, and other public settings. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LRR	First Aid Kit With Drug

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Special Storage Condition, Specify: Store at room temperature

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: eaf10b21-380e-4875-8982-2880ba0cdf5e
Public Version Date: July 23, 2019
Public Version Number: 1
DI Record Publish Date: July 15, 2019